BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BED

    MDR report key: 2902937 · Received November 29, 2012

    Report

    Report Number
    1824206-2012-07772
    Event Type
    Malfunction
    Date Received
    November 29, 2012
    Date of Event
    October 12, 2012
    Report Date
    October 12, 2012
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THAT THE SIDERAIL LATCH WAS DIRTY. HE CLEANED THE SIDERAIL LATCH MECHANISM AND THE SIDERAIL IS NOT FUNCTIONING PROPERLY.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THE LEFT FOOT SIDERAIL DOESN'T STAY UP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1